Matches in Nanopublications for { ?s ?p ?o <http://rdf.disgenet.org/resource/nanopub/NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance>. }
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- source_evidence_literature type ECO_0000212 NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- source_evidence_literature label "DisGeNET evidence - LITERATURE" NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- source_evidence_literature comment "Gene-disease associations inferred from text-mining the literature." NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_assertion description "[To further define the genetic basis of narcolepsy risk, we performed a genome-wide association study (GWAS) in 562 European individuals with narcolepsy (cases) and 702 ethnically matched controls, with independent replication in 370 cases and 495 controls, all heterozygous for DRB1*1501-DQB1*0602.]. Sentence from MEDLINE/PubMed, a database of the U.S. National Library of Medicine." NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_assertion evidence source_evidence_literature NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_assertion SIO_000772 20711174 NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_assertion wasDerivedFrom gad-20150221 NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_assertion wasGeneratedBy ECO_0000203 NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.
- gad-20150221 importedOn "2015-02-21" NP77963.RAAuEYxxAOKwClkviN3ZX7Hsp40IxNzCs5oJrqIunCk3U130_provenance.